Keywords: AD; autosomal dominant; ADNIV; autosomal dominant neovascular inflammatory vitreoretinopathy; AR; autosomal recessive; AR-1; autosomal recessive-1 allele identified; ARMS; amplification refractory mutation system; AZOOR; acute zonal occult outer retinopat
مقالات ISI (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Non-syndromic retinitis pigmentosa
Keywords: Retinitis pigmentosa; Rod-cone dystrophy; Inherited retinal dystrophy; Phenotype; Genotype-phenotype correlation; RP subtype; BBS; Bardet-Biedl syndrome; cGMP; cyclic guanosine monophosphate; CSNB; congenital stationary night blindness; ESCs; embryotic st
Genotype-functional-phenotype correlations in photoreceptor guanylate cyclase (GC-E) encoded by GUCY2D
Keywords: Cyclic GMP; Genotype-phenotype correlation; Guanylate cyclase; GUCY2D; Mutation; Photoreceptor; Retinal diseases; AAV; adeno-associated virus; ad; autosomal dominant; ar; autosomal recessive; BSP; bone spicule-like pigmentation; CCD; cyclase catalytic dom
TR3 is involved in hypoxia-induced apoptosis resistance in lung cancer cells downstream of HIF-1α
Keywords: NSCLC; non-small cell lung carcinoma; CsnB; cytosporone B; Hif-1α; hypoxia-inducible factor-1α; Non-small cell lung cancer; Hypoxia; Apoptosis; TR3; HIF-1α; Cytosporone B;
Pleiotropic effects of coat colour-associated mutations in humans, mice and other mammals
Keywords: αMSH; alpha-melanocyte-stimulating hormone; AS; Angelman syndrome; ATRN; Attractin (mahogany); ASIP; Agouti signalling protein; BLOC; Biogenesis of lysosomal organelles complex; CCSD; Canine congenital sensorineural deafness; CHS; Chediak-Higashi syndrom
Retinal horizontal cells reduced in a rat model of congenital stationary night blindness
Keywords: Retinal neurons; CSNB; Rat; Calbindin D-28K; Hereditary retinal disease;
A combustion concept for oxyfuel processes with low recirculation rate – Experimental validation
Keywords: Oxyfuel; Recirculation rate; CSNB; Experiments; Natural gas
Contribution of post-receporal cells to the cone a-wave of the human electroretinogram in congenital stationary night blindness and autoimmune-like retinopathy
Keywords: CSNB; Autoimmune retinopathy; Bipolar cells; Cone ERG a-wave;
Leber congenital amaurosis: Genes, proteins and disease mechanisms
Keywords: Animal models; Connecting cilium; Leber congenital amaurosis; Photoreceptors; Retina; Visual cycle; aa; amino acid; ACHM; achromatopsia; ad; autosomal dominant; ar; autosomal recessive; CSNB; congenital stationary night blindness; ERG; electroretinogram;